HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 5,10,15,20-tetrakis(4-ethynylphenyl)-21H,23H-Porphine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 5,10,15,20-Tetrakis[4-[2-(trimethylsilyl)ethynyl]phenyl]-21H,23H-porphine | HCID 135475294 | — |
| Solvent | Chloroform tetrahydrofuran | HCID 21956068 | — |
| Product | 5,10,15,20-tetrakis(4-ethynylphenyl)-21H,23H-Porphine | HCID 135999243 | — |
Reaction Steps
A solution of 700 mg (0.7 mmol) of protected TEPP (1) obtained above in 500 ml of a chloroform/tetrahydrofuran (THF) mixture (1/1 v/v) was cooled in a bath of liquid nitrogen and acetone to a temperature of between −30 and −50° C., and then a 1 mol/l solution of tetrabutylammonium fluoride (TBAF) in THF (259 mg, 0.99 mmol in 1 ml) was added to the reaction mixture, which was subsequently stirred for 20 hours. The rise in temperature was not controlled. The solvent was subsequently evaporated off and the deprotected porphyrin (2) was obtained in the form of a purple powder (747 mg, 1.05 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07919046B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-bae87a407f5a4e2f95a0b047939776bb |
| Source note | uspto-grants-2011_04 |